Tag: M.W=50-100

Puspitasari, W. C. published the artcileThe study of corrosion behaviour of intumescent fire retardant coating with structural steel substrate, Safety of 2-Methoxypropan-1-ol, the publication is International Journal of Electrochemical Science (2018), 13(10), 9916-9930, database is CAplus.

The aim of this work is to study corrosion behavior of intumescent coating and the primer on steel substrate before and after a fire test. The coated steel substrates were subjected to fire in a furnace at o 950° C for a vari able duration ranging from 30, 45, 90 and 120 min. All coated steel substrates were a lso subjected to corrosion test by immersing them in 5% NaCl solution, for 15 min and three months duration using Electrochem. Impedance Spectroscopy (EIS). The specimen’s impedance before fire test and before immersion was 4.37 × 108 cm². After 15 min exposure to NaCl, this value was reduced by 26, 53, 60 and 65% for specimens fired for 30, 45, 90 and 120 min, resp. Further reduction in the impedance by 97.6, 97.8, 97.9 and 98.9% for samples fired for 30, 45, 90 and 120 min, resp., were me asured after three months in 5% NaCl immersion.

International Journal of Electrochemical Science published new progress about 1589-47-5. 1589-47-5 belongs to ethers-buliding-blocks, auxiliary class Aliphatic hydrocarbon chain,Alcohol,Ether, name is 2-Methoxypropan-1-ol, and the molecular formula is C4H10O2, Safety of 2-Methoxypropan-1-ol.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Mortazavi, Saeideh-Sadat published the artcileA new Bronsted acid MIL-101(Cr) catalyst by tandem post-functionalization; synthesis and its catalytic application, Quality Control of 1589-47-5, the publication is Applied Organometallic Chemistry (2020), 34(8), e5717, database is CAplus.

A new heterogeneous Bronsted solid acid catalyst was prepared by tandem post-functionalization of MIL-101(Cr) and utilized for acetic acid esterification and alcoholysis of epoxides under solvent-free conditions. First, MIL-101(Cr) was functionalized with pyrazine to achieve MIL-101(Cr)-Pyz. Afterwards, the nucleophilic reaction of MIL-101(Cr)-Pyz with 1,3-propane sultone and next acidification with diluted sulfuric acid gave MIL-101(Cr)-Pyz-RSO₃H Bronsted solid acid catalyst. Various characterization methods such as Fourier transformation IR (FT-IR) spectroscopy, X-ray diffraction (XRD), elemental anal. (CHNS), XPS, SEM (SEM), energy-dispersive X-ray (EDX) spectroscopy, thermal anal. (TGA/DTA), acid-base titration, and N₂ adsorption/desorption anal. were employed to fully characterize the prepared catalyst. The catalyst showed high activity compared to unmodified MIL-101(Cr) in both catalytic acetic acid esterification and alcoholysis of epoxides. It can also be readily isolated from the reaction mixture and reused three times without major decrease in its activity.

Applied Organometallic Chemistry published new progress about 1589-47-5. 1589-47-5 belongs to ethers-buliding-blocks, auxiliary class Aliphatic hydrocarbon chain,Alcohol,Ether, name is 2-Methoxypropan-1-ol, and the molecular formula is C4H10O2, Quality Control of 1589-47-5.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Mortazavi, Saeideh-Sadat published the artcileInfluence of -SO₃H groups incorporated as Bronsted acidic parts by tandem post-synthetic functionalization on the catalytic behavior of MIL-101(Cr) MOF for methanolysis of styrene oxide, Name: 2-Methoxypropan-1-ol, the publication is Colloids and Surfaces, A: Physicochemical and Engineering Aspects (2020), 124703, database is CAplus.

Two kinds of Bronsted solid acid catalyst based on MIL-101(Cr) support were prepared by tandem post-synthetic functionalization. Covalent attachment of piperazine and DABCO (DABCO = 1,4 diazabicyclo[2.2.2]octane) followed by reaction with 1,3-propane sultone led to achieving MIL-pip-SO₃H and MIL-DABCO-SO₃H, resp. The obtained catalysts were characterized using several techniques which confirmed the presence of SO₃H groups in the MIL-101(Cr) framework. The catalytic behavior of the functionalized MIL-101(Cr) were evaluated and compared in the methanolysis of styrene oxide. Both solid acid catalysts showed superior catalytic efficiency compared to pristine MIL-101(Cr) under identical reaction conditions due to the presence of SO₃H groups, indicating the effect of post-synthetic modification on MIL-101(Cr) MOF.

Colloids and Surfaces, A: Physicochemical and Engineering Aspects published new progress about 1589-47-5. 1589-47-5 belongs to ethers-buliding-blocks, auxiliary class Aliphatic hydrocarbon chain,Alcohol,Ether, name is 2-Methoxypropan-1-ol, and the molecular formula is C4H10O2, Name: 2-Methoxypropan-1-ol.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Gharagheizi, Farhad published the artcileA New Neural Network Group Contribution Method for Estimation of Upper Flash Point of Pure Chemicals, Name: 2-Methoxypropan-1-ol, the publication is Industrial & Engineering Chemistry Research (2010), 49(24), 12685-12695, database is CAplus.

A new group contribution-based models is presented to predict the upper flash point temperature of pure compounds based on a large dataset (1294). This neural network model uses several occurrences of 122 chem. groups in a pure compound to predict its related upper flash point limit. The model squared correlation coefficient, average percent error, mean average error, and root-mean-square error over the main dataset (1294 pure compounds) were 0.99, 1.7%, 6, and 8.5, resp.

Industrial & Engineering Chemistry Research published new progress about 1589-47-5. 1589-47-5 belongs to ethers-buliding-blocks, auxiliary class Aliphatic hydrocarbon chain,Alcohol,Ether, name is 2-Methoxypropan-1-ol, and the molecular formula is C4H10O2, Name: 2-Methoxypropan-1-ol.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Ethers lack the hydroxyl groups of alcohols. Without the strongly polarized O―H bond, ether molecules cannot engage in hydrogen bonding with each other. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. Ethers do have nonbonding electron pairs on their oxygen atoms, however, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. Safety of 2-Methoxy-N-methylethanamine.

Zhang, Yu;Yang, Xinye;Yao, Qizheng;Ma, Dawei research published 《 CuI/DMPAO-Catalyzed N-Arylation of Acyclic Secondary Amines》, the research content is summarized as follows. DMPAO (I) has been found to be a powerful ligand to enable copper-catalyzed coupling of aryl halides with aliphatic acyclic secondary amines take place under relatively mild conditions, and coupling of aryl halides with primary amines and cyclic secondary amines proceeds at low catalyst loading.

Safety of 2-Methoxy-N-methylethanamine, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3. COA of Formula: C4H11NO.

Zhao, Hua;Martin, Caden J.;Larm, Nathaniel E.;Baker, Gary A.;Trujillo, Tyler C. research published 《 Enzyme activation by water-mimicking dual-functionalized ionic liquids》, the research content is summarized as follows. Biocatalytic synthesis represents a green alternative to metal-catalyzed reactions. However, enzymes typically display much lower catalytic activities in nonaqueous solvents than in aqueous media. To mimic the aqueous environment for enzyme activation, this study designed a series of sixteen dual-functionalized ionic liquids (ILs) that contain both glycol ether (hydrogen-bond acceptor) and tert-alc. (hydrogen-bond donor) groups. These “water-like” ILs enabled high transesterification activities for immobilized Candida antarctica lipase B (CALB) known as Novozym 435 and immobilized Bacillus licheniformis protease (known as subtilisin A), resp. Several water-mimicking ILs containing 2-3 vol% water significantly increased the CALB activity by 1.8-fold of that in tert-butanol, and 1.6-fold of that in diisopropyl ether (both organic solvents are highly enzyme-compatible). To a smaller degree, subtilisin was activated by these ionic solvents up to 1.2-fold (with 100% selectivity at 2 vol% water) than by diisopropyl ether. Fluorescence emission spectra suggested that the characteristic emission maximum peaks were maintained in “water-like” ILs in most cases.

COA of Formula: C4H11NO, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers lack the hydroxyl groups of alcohols. Without the strongly polarized O―H bond, ether molecules cannot engage in hydrogen bonding with each other. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. Ethers do have nonbonding electron pairs on their oxygen atoms, however, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. Application of C4H11NO.

Zhao, Junjun;Gou, Shaohua;Zhang, Xiaobing;Liang, Yan;Fang, Lei research published 《 Novel [1,2,4] Triazol [4,3-a] Pyridine Derivatives as Potential Selective c-Met Inhibitors with Improved Pharmacokinetic Properties》, the research content is summarized as follows. Total twenty-nine [1,2,4]triazolo[4,3-a]pyrazine derivatives were designed and synthesized. The target compounds, especially 4aa, showed potent activity to inhibit c-Met both in an enzyme assay and a cellular assay. The comprehensive screening for the inhibition of 60 different kinases revealed that 4aa could selectively inhibit c-Met while had no effect on other kinases, indicating 4aa is an excellent c-Met selective inhibitor. The flow cytometry studies found that 4aa had a similar behavior to the pos. control SGX-523 in terms of causing the tumor cell apoptosis and blocking cell-cycle progression. More importantly, 4aa showed much better pharmacokinetic properties than SGX-523. Altogether, the findings suggested the target compounds may be potential anti-tumor drug candidates.

Application of C4H11NO, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers do have nonbonding electron pairs on their oxygen atoms, 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds. Quality Control of 38256-93-8.

Zhou, Jingwei;Li, Lamei;Wang, Songping;Yan, Ming;Wei, Wentao research published 《 Catalyst-free photodecarbonylation of ortho-amino benzaldehydes》, the research content is summarized as follows. A catalyst-free photodecarbonylation of the aldehydes I (R = H, 2-F, 4-Br, 3-CN, etc.; R¹ = Me, Et, n-Bu, Bn; R² = Me, prop-2-en-1-yl, Bn, etc.; R¹R² = -(CH₂)₄-, -(CH₂)₅-, -(CH₂)₆-, etc.) based on the conformational-selectivity design strategy has been discovered. It revealed that decarbonylation can be easily achieved with visible light irradiation by introducing a tertiary amine into the ortho-position of the aldehyde group. A diverse array of tertiary amines II is tolerated by our photodecarbonylation under mild conditions. Furthermore, the (QM) computations of the mechanism and the experiments on well-designed special substrates revealed that our photodecarbonylation depends on the conformational specificity of the aldehyde group and tertiary amine, and occurs through an unusual [1,4]-H shift and a subsequent [1,3]-H shift.

38256-93-8, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., Quality Control of 38256-93-8

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers are a class of organic compounds that contain an ether group—an oxygen atom connected to two alkyl or aryl groups. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine.They have the general formula R–O–R′, where R and R′ represent the alkyl or aryl groups. Related Products of 38256-93-8.

Zhou, Jingwei;Wang, Songping;Duan, Wentao;Lian, Qi;Wei, Wentao research published 《 Catalyst-free photoinduced selective oxidative C(sp³)-C(sp³) bond cleavage in arylamines》, the research content is summarized as follows. Due to the directional nature of sp³-hybridized orbitals and the absence of π-orbitals, the oxidative cleavage of the kinetically and thermodynamically stable C(sp³)-C(sp³) bond is extremely difficult and remains scarcely explored. In this work, under the double argument of quantum mechanics (QM) computations and meticulous experiments on authors’ well-designed C-C single bond cleavage mechanism, authors discovered a means of photoinduced selective oxidative C(sp³)-C(sp³) bond cleavage in arylamines, easily achieved by simple visible light irradiation using O₂ as a benign oxidant under very mild conditions. The utility of methodol. was demonstrated by the C(sp³)-C(sp³) bond cleavage in morpholine/piperazine arylamines with excellent functional group tolerance. Importantly, this methodol. is noteworthy, not only it does not require any catalysts, but also it provides valuable possibilities for the scalable functionalization of clin. drugs and natural products.

38256-93-8, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., Related Products of 38256-93-8

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers can again be classified into two varieties: if the alkyl or aryl groups are the same on both sides of the oxygen atom, 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine. Then it is a simple or symmetrical ether, whereas if they are different, the ethers are called mixed or unsymmetrical ethers. Name: 2-Methoxy-N-methylethanamine.

Zhou, Yuntao;Ye, Hebo;You, Lei research published 《 Reactivity-Based Dynamic Covalent Chemistry: Reversible Binding and Chirality Discrimination of Monoalcohols》, the research content is summarized as follows. In an effort to develop reactivity-based dynamic covalent bonding and to expand the scope and application of the dynamic covalent chem., in situ-generated simple generic iminium ions were utilized for the dynamic covalent binding of monoalcs. with high affinity. Hammett anal. was conducted to manipulate the equilibrium and correlate with the reactivity of reactants. The structural features of aldehydes and secondary amines were identified, and both polar and steric effects have significant impact on the binding. In particular, the substrates which can participate in π-π and polar-π interactions are able to afford apparent equilibrium constants in the magnitude of 10⁴ M^-2, demonstrating the power of weak supramol. forces to stabilize the dynamic covalent assembly. The generality of the assembly was validated with a series of mono secondary alcs. To showcase the practicality of our system, chirality discrimination and ee measurement of chiral secondary alcs. were achieved.

38256-93-8, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., Name: 2-Methoxy-N-methylethanamine

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem